Use of a preparation of cimicifuga racemosa

ABSTRACT

A preparation of  Cimicifuga racemosa  can be used to successfully treat urinary incontinence in female mammals following an ovariohysterectomy. Positive results can be expected for the treatment of women following a hysterectomy or after the menopause.

[0001] The invention relates to the use of a preparation of Cimicifuga racemosa (Black Snakeroot), in particular an extract thereof, and more particularly an extract of the rhizome (Rhizoma cimicifugae racemosae).

[0002] Extracts of Cimicifuga racemosa are used in gyniatrics for the treatment of menopause complaints, such as hot flushes, sweating, sleep disorders, irritability, and depressive disgruntlement. The extract is regarded as a phytosubstitute for oestrogen replacement therapy. Extracts of Cimicifuga racemosa play no significant role in allopathic veterinary medicine.

[0003] It has been found, surprisingly, that preparations of Cimicifuga racemosa are therapeutically effective against urinary incontinence.

[0004] It is known that approximately 20% of bitches which have been subjected to castration, ie excision of the ovaries, and possibly also of the uterus, suffer from urinary incontinence as a secondary symptom of the operation after the elapse of approximately 2.7 years on average following ovariohysterectomy. The clinical symptoms are nowadays primarily treated with sympathomimetics, which, however, cause serious side effects in animals not optimally adjusted.

[0005] It was formerly assumed that this urinary incontinence was a result of the oestrogen deficiency induced by the operation. Despite doubts concerning such causality, aroused by the fact that the clinical picture does not occur prior to an elapse of an average of 2.7 years following ovariectomy, attempts have been made to treat the symptoms by oestrogen replacement. These doubts, combined with the side effects occurring during therapy have led to increased consideration of effecting treatment with sympathomimetics.

[0006] In women over 60 and having a basal incontinence incidence of from 10 to 33%, hysterectomy, ie the removal of the uterus but not the ovaries, ie without additionally influencing the hormonal status, raises the probability of developing urinary incontinence by 60%. Lesions caused by the operation on nerves and ligamentary connective tissue structures in the pelvic region are under discussion as being the cause of the problem (Lancet 2000; 356(9229): 535-539). Lesions of the same kind also commonly occur with the operative technique typically used in veterinary medicine. The effectiveness of the preparation of Cimicifuga racemosa of the invention for the treatment of urinary incontinence is thus not based on the properties hitherto ascribed to Cimicifuga racemosa as oestrogen substitute or as endocrinally active phytotherapeutic but rather on effects beyond known properties.

[0007] Although one must be cautious when considering applying veterinary causal and therapeutic findings to human syndromes, the results found suggest efficacy for the treatment of urinary incontinence in ovariectomized women or permenopausal or postmenopausal women. The occurrence of urinary incontinence in postmenopausal women is between 20 and 50% depending on age. No increase is observed in the perimenopause. Early oestrogen replacement is associated with slight symptom improvement on a short term basis only, whilst in the long run it is associated with an increase in the incontinence risk in women over 60, as has been shown in a published study (D. H. Thom, J. S. Brown in J. Am. Geriatr. Soc. 1998; 46(11): 1411-1417).

[0008] Thus the prior state of knowledge could not have suggested the presently proposed use of Cimicifuga racemosa for treatment of urinary incontinence and is unable to provide an explanation of the observed success thereof.

[0009] An effective daily dosage for the application proposed by the invention has been found to be a drug content of between 0.1 and 10 mg/kg of body weight. Thus it is advantageous to formulate an extract as tablets having a drug content of between 5 and 200 mg, and preferably between 10 and 50 mg, per tablet.

[0010] In the present invention, it is preferred to use an extract which has been prepared using an alcoholic extracting agent, particularly ethanol, isopropanol, or methanol.

[0011] Administration can be accomplished using any of the commonly used pharmaceutical administration forms, such as granules, capsules, suppositories, tablets, solutions, tea preparations, or by transdermal means, such as a plaster or the like.

[0012] It is also suitable as an additive for food or fodder.

[0013] The preparation must not necessarily be administered as an extract For example, it is possible to grind the plant or portions thereof for direct or indirect ingestion, for example, as tea.

[0014] Therapy involving the preparation of Cimicifuga racemosa as proposed in the invention is particularly suitably for female mammals following an ovariohysterectomy and for women following a hysterectomy or after the menopause.

EXAMPLE

[0015] Ovariectomized bitches showing the symptomatic complex of urinary incontinence were treated with an extract of Rhizoma cimicifugae racemosae in the form of tablets (“Remlfemin” tablets, sold by Schaper & Brummer GmbH & Co. KG). An effective daily intake of from one half to one whole tablet per 10 kg of body weight was used. In all of the fourteen cases treated there was remittence of the incontinence. The subjective judgement of the owners of the treated bitches on the therapeutic success and the compatibility of the pharmaceutical preparation was positive in all cases. In all cases, the owners asked for continuation of the therapy. In all cases there was distinct improvement of condition going, in some cases, as far as complete subsidence of the complaint.

[0016] The Remifemin® tablets used contain an extract of 20 mg of drug per tablet. The extracting agent used was isopropanol 40 vol %. 

1. The use of a preparation of Cimicifuga racemosa for treatment of urinary incontinence.
 2. The use of an extract of Cimicifuga racemosa as claimed in claim
 1. 3. The use of an extract as claimed in claim 2 which has been produced using an alcoholic extracting agent.
 4. The use of an extract as claimed in claim 2 or claim 3 in the form of tablets having a drug content of between 5 and 200 mg per tablet.
 5. The use of a preparation as claimed in any one of claims 1 to 4 as an additive for supplemented fodder. 